DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
|
25012701 |
2015 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
|
24949729 |
2014 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
|
24949729 |
2014 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Analysis of trafficking, stability and function of human connexin 26 gap junction channels with deafness-causing mutations in the fourth transmembrane helix.
|
23967136 |
2013 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Analysis of trafficking, stability and function of human connexin 26 gap junction channels with deafness-causing mutations in the fourth transmembrane helix.
|
23967136 |
2013 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
|
22695344 |
2012 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness].
|
22567861 |
2012 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
|
22695344 |
2012 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness].
|
22567861 |
2012 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Multiple effects of childhood deafness on cortical activity in children receiving bilateral cochlear implants simultaneously.
|
21094084 |
2011 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Multiple effects of childhood deafness on cortical activity in children receiving bilateral cochlear implants simultaneously.
|
21094084 |
2011 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
[Mutation of Gap junction protein beta 2 gene and treatment outcome of cochlear implantation in cochlear implantation recipients].
|
19567088 |
2009 |
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
[Mutation of Gap junction protein beta 2 gene and treatment outcome of cochlear implantation in cochlear implantation recipients].
|
19567088 |
2009 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
GeneticVariation
|
CLINVAR |
GJB2: the spectrum of deafness-causing allele variants and their phenotype.
|
15365987 |
2004 |
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
|
|
0.700 |
CausalMutation
|
CLINVAR |
|
|
|